Product NDC: | 52584-025 |
Proprietary Name: | Sodium Chloride |
Non Proprietary Name: | Sodium Chloride |
Active Ingredient(s): | 234 mg/30mL & nbsp; Sodium Chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-025 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20111026 |
Package NDC: | 52584-025-30 |
Package Description: | 1 VIAL in 1 BAG (52584-025-30) > 30 mL in 1 VIAL |
NDC Code | 52584-025-30 |
Proprietary Name | Sodium Chloride |
Package Description | 1 VIAL in 1 BAG (52584-025-30) > 30 mL in 1 VIAL |
Product NDC | 52584-025 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Chloride |
Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
Route Name | INTRAVENOUS |
Start Marketing Date | 20111026 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | SODIUM CHLORIDE |
Strength Number | 234 |
Strength Unit | mg/30mL |
Pharmaceutical Classes |